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Regulatory and Quality Compliance Support

Active

Federal

Response Deadline08/24/2026, 05:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

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This subcontract opportunity, titled Regulatory and Quality Compliance Support, is issued by the Department of Defense under the Medical Supply Chain Pharm FSA. The primary objective is to provide comprehensive regulatory and quality compliance support to ensure that all products, packaging, and documentation adhere to DLA, FDA, OSHA, and DFARS requirements. Key responsibilities include managing shelf-life tracking and maintaining constant audit readiness. The procurement is categorized under NAICS code 541611 and is set for performance in APO 09865-0061. Interested parties must submit their responses by the deadline of August 24, 2026, following the posting date of August 16, 2026.

General Info

DoD subcontract for regulatory and quality compliance support, due by August 24, 2026.

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSAView Agency

NAICS

541611 - Administrative Management and General Management Consulting ServicesView NAICS

Place of Performance

APO, AE, 09865-0061, USA

Set-Aside

NONE

Documents

This scope was carved out of SPE2DP-26-T-4655.

The full solicitation package (1 document), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

REHYDRATION SALTS FOR

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Timeline

PostedAug 16

subcontract

Response DeadlineAug 24

Submission deadline

Response Deadline

08/24/2026, 05:00:00 PM UTCin 7 days

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

ContactsNo contacts available

OfficeN/A

Organization / Agency

Department Of Defense → MEDICAL SUPPLY CHAIN PHARM FSA

View Agency Profile

Office AddressN/A

ContactsNo contact information available

Full Description

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Provide regulatory and quality compliance support to ensure product, packaging, and documentation meet DLA, FDA, OSHA, and DFARS requirements, including shelf-life tracking and audit readiness.

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